14
Electromagn. compatibility:
Device fulfils the stipulations of the European standard EN 60601-1-2
Device fulfils the stipulations of the European standard EN 60601-1-2
Clinical testing:
The clinical performance test was carried out in Germany according to the DIN 58130 / 1997
The clinical performance test was carried out in Germany according to the DIN 58130 / 1997
procedure N6 (sequential).
The stipulations of the EU-Guidelines 93/42/EWG for Medical Products Class IIa have been fulfilled.
The stipulations of the EU-Guidelines 93/42/EWG for Medical Products Class IIa have been fulfilled.
9. Technical specifications
9. Technical specifications
Weight:
145g (with bat cuff)
Size:
80 x 70 x 75mm (including cuff)
Storage temperature:
–5 to +50°C
Humidity:
15 to 85% relative humidity maximum
Operation temperature:
10 to 40°С
Display:
LCD-Display (Liquid Crystal Display)
Measuring method:
oscillometric
Measuring range:
- SYS/DIA
30 to 280 mmHg
- pulse
40 to 200 per minute
Cuff pressure display range:
0 to 299 mmHg
Memory:
storing the last 30 measurements automatically
Measuring resolution:
1 mmHg
Accuracy:
- pressure
within ±3 mmHg
- pulse
>5 % of the reading
Power source:
2 dry cells (Batteries) UM-4, size AAA 1.5V
Accessories:
storage case, 2 dry cells (Batteries) UM-4, size AAA,
instruction manual
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